4,5-Dihydroorotic acid

4,5-Dihydroorotic acid
Names

IUPAC name 2,6-dioxo-1,3-diazinane-4-carboxylic acid
Identifiers
CAS Number	155-54-4^N
ChEBI	CHEBI:30865^Y
ChEMBL	ChEMBL75782^Y
ChemSpider	628^Y
Jmol interactive 3D	Image
MeSH	4,5-dihydroorotic+acid
PubChem	648
InChI InChI=1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11)^Y Key: UFIVEPVSAGBUSI-UHFFFAOYSA-N^Y InChI=1/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11) Key: UFIVEPVSAGBUSI-UHFFFAOYAI
SMILES O=C1NC(=O)NC(C(=O)O)C1
Properties
Chemical formula	C₅H₆N₂O₄
Molar mass	158.112 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

4,5-Dihydroorotic acid is a derivative of orotic acid which serves as an intermediate in pyrimidine biosynthesis.^[1]

References

↑ Francois Lacroute (March 1968). "Regulation of Pyrimidine Biosynthesis in Saccharomyces cerevisiae1". J. Bacteriol. 95: 824–832.

Nucleotide metabolic intermediates

Purine metabolism

Anabolism

R5P→IMP:	R5P PRPP PRA GAR FGAR FGAM AIR CAIR SAICAR AICAR FAICAR

IMP→AMP:	Adenylosuccinate

IMP→GMP:	Xanthosine monophosphate

Catabolism

Pyrimidine metabolism

Anabolism

Catabolism

uracil:	Dihydrouracil 3-Ureidopropionic acid β-Alanine

thymine:	Dihydrothymine β-Ureidoisobutyric acid 3-Aminoisobutyric acid

This article is issued from Wikipedia - version of the Tuesday, March 17, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.